• 한국표면공학회지
• /
• 제30권5호
• /
• pp.333-346
• /
• 1997

Plasma spray processes for functional coatings of tubular SOFC ( Soild oxide Fuel Cell).consisting of air electrode, oxide electrolyte, an fuel electrode, are optimized by fully saturated fractional factorial testing. Material and electric characteristics of each coating are analtsed by the implementation of SEM and optical microscope for evaluating microstructure and porosity, X-ray diffraction method for investigating compositional change between raw powder and sprayed coating, and Van der Pauw method for measuring electrical conductivity. LSM ($La_{0.65}Sr_{0.35}MnO_3$air electrode and Ni-YSL fuel electrode coatings have porosities of around 23~30% sufficient for effective fuel and oxidant gas supply to electrochemical reaction interfaces and electrical conductivities of around 90 S/cm and 1000 S/cm, respectively, enough for acting as current collecting electrodes. YSZ($ZrO_2-8mol%Y_2O_3$) electrolyte film has a high ionic conductivities of 0.05~0.07 S/cm at $1000^{\circ}C$ in air atmosphere, but appears to be somewhat too porous to reduce the thickness. for enhancing the cell efficiency. A unit tubular SOFC has beem fabricated by the optimized plasma spray processes for each functional coating and the cell. Its electrochemical chracteristics are investigated by measuring voltage-current and power density with variation of operationg temperature, radio of fuel to air gas flowrates, and total gas flowrate of reactants.

• Journal of Electrochemical Science and Technology
• /
• 제8권2호
• /
• pp.101-106
• /
• 2017

$Li_2SiO_3$ was used as a coating material to improve the electrochemical performance of $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$. $Li_2SiO_3$ is not only a stable oxide but also an ionic conductor and can, therefore, facilitate the movement of lithium ions at the cathode/electrolyte interface. The surface of the $Li_2SiO_3$-coated $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ was covered with island-type $Li_2SiO_3$ particles, and the coating process did not affect the structural integrity of the $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ powder. The $Li_2SiO_3$ coating improved the discharge capacity and rate capability; moreover, the $Li_2SiO_3$-coated electrodes showed reduced impedance values. The surface of the lithium-ion battery cathode is typically attacked by the HF-containing electrolyte, which forms an undesired surface layer that hinders the movement of lithium ions and electrons. However, the $Li_2SiO_3$ coating layer can prevent the undesired side reactions between the cathode surface and the electrolyte, thus enhancing the rate capability and discharge capacity. The thermal stability of $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ was also improved by the $Li_2SiO_3$ coating.

• 한국세라믹학회지
• /
• 제37권7호
• /
• pp.705-712
• /
• 2000

In this study, the dispersion stability of CeO2 based complex oxide was studied, and density, porosity, and microstructure of green body were investigated using colloid surface chemistry to manufacture the Gd2O3 doped CeO2 solid electrolyte in an aqueous system. To prepare the stable slurry for slip casting, the dispersion stability was examined as a function of pH using ESA(electrokinetic sonic anplitude) analysis. The dynamic mobility of particles was enhanced with anionic and cationic dispersant were added the amount of 0.5wt% respectively, but pH value in slurries didn't move to below 6.0 because of the influence of dopants. This phenomenon also appeared in the CeO2-Y2O3 and CeO2-Sm2O3 systems, so it could be inferred that rare earth dopants such as Gd2O3, Sm2O3 and Y2O3 not only have the similar motion with changing pH in an aqueous system but also can be dissolved in the range of pH 6.0∼6.5. In CeO2-Gd2O3 system, when the anionic dispersant was added the amount of 0.5wt% and pH value in slurries was fixed at 9.5, the green body density was 4.07g/㎤, and the relative density of sintered body was 95.2%. It could be inferred from XRD analysis that Gd3+ substituted into Ce4+ site because there was no free Gd2O3 peak.

• 에너지공학
• /
• 제19권2호
• /
• pp.73-80
• /
• 2010

고체산화물연료전지(SOFC)는 청정에너지기술로써 화학에너지를 전기에너지로 직접 전환한다. SOFC는 열병합발전과 결합하여 80%이상의 효율을 올릴 수 있으며 천연가스와 바이오가스 등 연료에 대한 융통성이 폴리머전해질막연료전지(PEMFC)보다 높다. YSZ전해질과 함께 SOFC에 주로 채용되는 공기극 재료는 아직까지 Sr이 첨가된 $LaMnO_3$(LSM)이다. LSM 이외에, 혼합전도성을 가지는 페로브스카이트로서 Sr첨가 $LaCoO_3$(LSCo), $LaFeO_3$(LSF), $LaFe_{0.8}Co_{0.2}O_3$(LSCF)는 공기극 임피던스가 LSM에 비해 현저히 낮아 연구가 증가하고 있다. 그러나 SOFC전극의 소결온도에서 YSZ과 고체반응을 일으키는 문제점과 열팽창 계수가 YSZ와 격차가 크게 나는 문제점 때문에 전극 제조가 복잡하다. 따라서 전해질과의 화학적 안정성 및 유사한 열팽창계수(TEC)를 가지면서 우수한 전기화학활성을 제공하는 것이 해결해야할 중요한 문제로 남는다.

• 한국응용과학기술학회지
• /
• 제36권1호
• /
• pp.200-207
• /
• 2019

본 연구에서는 "이온젤"이라고 불리는 고분자 기반의 PVA(polyvinyl alcohol)-$H_3PO_4$의 고체 전해질에 이온성 액체 $BMIMBF_4$ (1-buthyl-3-methylimidazolium tetrafluoroborate)를 첨가하여 제조한 전고체 전해질과 환원된 그래핀 옥사이드/전도성 고분자 복합재료 기반의 전극 재료를 이용하여 유연성을 갖는 슈퍼커패시터를 제작 하였으며, 유연성에 따른 전기화학적 특성을 분석하여 보았다. 환원된 그래핀 옥사이드/전도성 고분자 복합재료와 전고체 전해질 기반의 유연성 슈퍼커패시터의 전기화학적 특성을 유연성에 따라서 측정하기 위해서 프레스로 $0.01kg/cm^2$의 일정한 압력으로 최대 100회 까지 굽힘 시험(bending test)을 진행 하였으며, 0~100 회의 굽힘 시험 이후에 순환 전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충 방전법(GCD)을 통하여 비교 및 분석하여 보았다. 그 결과로, 유연성 슈퍼커패시터의 초기 전기용량은 43.9 F/g으로 확인 할 수 있었고, 이 값은 50회, 100회의 굽힘 시험 후에 각각 42.0F/g, 40.1F/g로 감소하는 현상을 확인할 수 있었다. 이러한 결과로 미루어 보아 물리적인 응력이 슈퍼 커패시터의 전기화학적 특성 감소에 영향을 주는 것으로 사료되며 또한, 굽힘 횟수에 따른 슈퍼커패시터의 전기화학적 특성 감소 원인을 확인하기 위해서 굽힘 시험 전과 후의 전극표면을 전자주사 현미경으로 관찰하여 보았다.

• 한국전기전자재료학회:학술대회논문집
• /
• 한국전기전자재료학회 2006년도 추계학술대회 논문집 Vol.19
• /
• pp.304-304
• /
• 2006

Ternary tellurite glassy systems ($Li_2O-V_2O_5-TeO_2$) have been synthesised using Vanadium oxide as a network former and Lithium oxide as network modifier. The addition of a metal oxide makes them electric or mixed electric-ionic conductors, which are of potential interest as cathode materials for solid-state batteries. This glass-ceramics crystallized from the $Li_2O-V_2O_5-TeO_2$ system are particularly interesting, because they exhibit high conductivity (up to $5.63{\times}10^{-5}$ S/cm) at room temperature the glass samples were prepared by quenching the melt on the copper plate and the glass-ceramics were heat-treated at crystallizing temperature determined from differential thermal analysis (DTA). The electric DC conductivity result have been analyzed in terms of a small polaron-hopping model.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
• /
• pp.478.2-478.2
• /
• 2014

Atomic layer deposition (ALD) provides self-limiting processes based on chemisorption-based reactions. Such unique features allow for superior step coverage, atomic-scale control in thickness, and surface-dependent reaction controls. Furthermore, the surface-limited deposition enables the artificial deposition of oxide and/or metallic materials onto the porous systems as long as the supply is guaranteed in terms of time in providing reactant species and removing the byproducts and redundant reactants. The unique feature of atomic layer deposition is applied to solid oxide fuel cells whose incorporates two porous cathode and anode compartments in addition to the ionic electrolyte. Specific materials are deposited to the surface sites of porous electrodes, with the aim to controlling the triple phase boundaries crucial for the optimized SOFC performances. The effect of ALD on the SOFC performance is characterized using current-voltage characteristics in addition to frequency-dependent impedance spectroscopy. The pros and cons of ALD-controlled SOFCs are discussed toward high-performance SOFC systems.

• 한국전기전자재료학회:학술대회논문집
• /
• 한국전기전자재료학회 2005년도 하계학술대회 논문집 Vol.6
• /
• pp.334-335
• /
• 2005

Ternary tellurite glassy systems ($Li_2O-V_2O_5-P_2O_5$) have been synthesised using Vanadium oxide as a network former and Lithium oxide as network modifier. The addition of a metal? oxide makes them electric or mixed electric-ionic conductors, which are of potential interest as cathode' materials for solid-state batteries. This glass-ceramics crystallized from the $Li_2O-V_2O_5-P_2O_5$ system are particularly interesting, because they exhibit high conductivity (up to $5.95\times10^{-4}$ S/cm) at room temperature. the glass samples were prepared by quenching the melt on the copper plate and the glass-ceramics were heat-treated at crystallizing temperature determined from differential thermal analysis (DTA). The electric D.C conductivity result have been analyzed in terms of a small polaron-hopping model.

• 대한전기학회:학술대회논문집
• /
• 대한전기학회 1999년도 하계학술대회 논문집 D
• /
• pp.1547-1549
• /
• 1999

As a preliminary experiment for the development of anode-supported tubular cell with proper porosity, we have investigated the anode substrate and the electrolyte-coated anode tube. The anode substrate was manufactured as a function of carbon content in the range of 20 to 50 vol.%. As the caron content increased, the porosity of the anode substrate increased slightly and the carbon content with proper porosity was obtained at 30 vol.%. The anode tube was fabricated by extrusion process and the electrolyte layer was coated on the anode tube by slurry dipping process. The anode-supported tube was cofired successfully. Their sintered property and microstructure were examined and the porosity of the anode tube was 35%. From the gas permeation test, the anode tube was found to be porous enough for gas supply. On the other hand, the anode-supported tube with electrolyte layer indicated a very low gas permeation rate. This means that the coated electrolyte was dense. Based upon these experimental results. we will fabricate and test the anode-supported tubular cell.

• 한국세라믹학회지
• /
• 제43권12호
• /
• pp.788-797
• /
• 2006

An anode-supported SOFC single cell having $5{\mu}m$ thin electrolyte was fabricated cost-effectively by tape casting, laminating, and co-filing of anode (NiO-YSZ), cathode (LSM-YSZ), and electrolyte (YSZ) components. The optimal slurry compositions of the green tapes for SOFC components were determined by an analysis of the mean diameter, the slurry viscosity, the tensile strength/strain of the green tapes, and their green microstructures. The single cells with a dense electrolyte and porous electrodes could be co-fired successfully at $1325\sim1350^{\circ}C$ by controlling the contents of pore former and the ratio of coarse YSZ and fine YSZ in the anode and the cathode. The single cell co-fired at $1350^{\circ}C$ showed $100.2mWcm^{-2}$ of maximum power density at $800^{\circ}C$ but it was impossible to apply it to operate at low temperature because of low performance and high ASR, which were attributed to formation of the secondary phases in the cathode and the interface between the electrolyte and the cathode.